CREM Co Labs Announces Breakthrough Publication in ACS Synthetic Biology

We are pleased to announce that our latest peer-reviewed research article, “Construction and Functional Characterization of a Heterologous Quorum Sensing Circuit in Clostridium sporogenes,” has been officially published in ACS Synthetic Biology.

Full text: https://pubs.acs.org/doi/full/10.1021/acssynbio.5c00628

This work represents a significant milestone for CREM Co Labs. For the first time, we successfully engineered a functional, peptide-based quorum sensing (QS) system, originally from Staphylococcus aureus, into the obligate anaerobe Clostridium sporogenes, a leading candidate for tumor-targeted bacterial therapies.

Why This Breakthrough Matters

Our research demonstrates:

  • Successful integration of the agr QS operon from S. aureus into C. sporogenes, enabling density-dependent gene activation.

  • Precise control over gene expression, confirmed through LC-MS/MS quantification of AIP-III and GFP reporter kinetics.

  • Signal specificity and cross-inhibition, showing that C. sporogenes can discriminate between cognate and non-cognate AIPs, critical for multiplexed synthetic-biology control circuits.

  • Population-threshold activation behavior, allowing engineered bacteria to turn on therapeutic functions only when they reach sufficient density in targeted environments such as tumors.

    Advancing CREM’s Bacteria-Mediated Cancer Therapy Platform

    This publication establishes a foundational regulatory system that will allow future therapeutic C. sporogenes strains to:

    • Activate engineered therapeutic genes only inside the hypoxic tumor microenvironment,

    • Release anti-cancer payloads at controlled population thresholds, and

    • Improve safety, precision, and tumor specificity in next-generation oncolytic bacterial therapies.

    This is a major step forward for CREM Co Labs’ long-term vision of intelligent, programmable microbial therapeutics.

     Acknowledgements

    We acknowledge our co-authors Dr. Brian Ingalls, Dr. Marc Aucoin, and Dr. Sara Sadr from University of Waterloo, and we thank MITACS for supporting this research through a partnership with CREM Co Labs.